Browsing Universitätsbibliographie by Author "Mau-Holzmann, Ulrike A."

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A Case Study from the Past: The RGC-5 vs. the 661W Cell Line: Similarities, Differences and Contradictions-Are They Really the Same?

Hurst, Jose; Attrodt, Gesine; Bartz-Schmidt, Karl-Ulrich; Mau-Holzmann, Ulrike Angelika; Spitzer, Martin Stephan; Schnichels, Sven (2023)
A Mouse Bone Marrow Stromal Cell Line with Skeletal Stem Cell Characteristics to Study Osteogenesis In Vitro and In Vivo

Raeth, Sebastian; Sacchetti, Benedetto; Siegel, Georg; Mau-Holzmann, Ulrike A.; Hansmann, Jan; Vacun, Gabriele; Hauk, Thomas G.; Pfizenmaier, Klaus; Hausser, Angelika (2014)
Alternative splicing of the tumor suppressor ASPP2 results in a stress-inducible, oncogenic isoform prevalent in acute leukemia

Schittenhelm, Marcus Matthias; Walter, Bianca; Tsintari, Vasileia; Federmann, Birgit; Saipi, Mihada Bajrami; Akmut, Figen; Illing, Barbara; Mau-Holzmann, Ulrike; Fend, Falko; Lopez, Charles Darin; Kampa-Schittenhelm, Kerstin Maria (2019)
Amniotic bands as a cause of congenital anterior staphyloma

Schramm, Charlotte; Rohrbach, Jens M.; Reinert, Siegmar; Mau-Holzmann, Ulrike A.; Aisenbrey, Sabine; Bartz-Schmidt, Karl-Ulrich; Besch, Dorothea (2013)
Characterisation of the Cell Line HC-AFW1 Derived from a Pediatric Hepatocellular Carcinoma

Armeanu-Ebinger, Sorin; Wenz, Julia; Seitz, Guido; Leuschner, Ivo; Handgretinger, Rupert; Mau-Holzmann, Ulrike A.; Bonin, Michael; Sipos, Bence; Fuchs, Joerg; Warmann, Steven W. (2012)
Discordance between ultrasound and cell free DNA screening for monosomy X

Kagan, Karl Oliver; Hoopmann, Markus; Singer, Sylke; Schaeferhoff, Karin; Dufke, Andreas; Mau-Holzmann, Ulrike A. (2016)
Epigenetic activation of O-linked beta-N-acetylglucosamine transferase overrides the differentiation blockage in acute leukemia

Kampa-Schittenhelm, K. M.; Haverkamp, T.; Bonin, M.; Tsintari, V; Buehring, H. J.; Haeusser, L.; Blumenstock, G.; Dreher, S. T.; Ganief, T.; Akmut, F.; Illing, B.; Mau-Holzmann, U. A.; Bonzheim, I; Schleicher, E.; Vogel, W.; Schittenhelm, M. M. (2020)
Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutation

Schwarz, Niklas; Uysal, Betuel; Rosa, Filip; Loeffler, Heidi; Mau-Holzmann, Ulrike A.; Liebau, Stefan; Lerche, Holger (2019)
First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study

Kagan, Karl Oliver; Hoopmann, Markus; Pfaff, Theresa; Prodan, Natalia; Wagner, Philipp; Schmid, Maximilian; Dufke, Andreas; Mau-Holzmann, Ulrike; Brucker, Sara; Marcato, Livia; Malvestiti, Barbara; Grati, Francesca Romana (2020)
Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS plus carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p. Leu46Met) mutation

Haag, Carolin; Uysal, Betuel; Marquetand, Justus; Loeffler, Heidi; Mau-Holzmann, Ulrike A.; Lerche, Holger; Schwarz, Niklas (2023)
Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H196

Marthaler, Adele G.; Schmid, Benjamin; Tubsuwan, Alisa; Poulsen, Ulla B.; Engelbrecht, Alexander F.; Mau-Holzmann, Ulrike A.; Hyttel, Poul; Nielsen, Jorgen E.; Nielsen, Troels T.; Holst, Bjorn (2016)
Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H266

Marthaler, Adele G.; Tubsuwan, Alisa; Schmid, Benjamin; Poulsen, Ulla B.; Engelbrecht, Alexander F.; Mau-Holzmann, Ulrike A.; Hyttel, Poul; Nielsen, Troels T.; Nielsen, Jorgen E.; Holst, Bjorn (2016)
Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H271

Marthaler, Adele G.; Schmid, Benjamin; Tubsuwan, Alisa; Poulsen, Ulla B.; Engelbrecht, Alexander F.; Mau-Holzmann, Ulrike A.; Hyttel, Poul; Nielsen, Jorgen E.; Nielsen, Troels T.; Holst, Bjorn (2016)
Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein tau (MAPT) gene

Nimsanor, Natakarn; Poulsena, Ulla; Rasmussen, Mikkel A.; Clausen, Christian; Mau-Holzmann, Ulrike A.; Nielsen, Jorgen E.; Nielsen, Troels T.; Hyttel, Poul; Holst, Bjorn; Schmid, Benjamin (2016)
Generation of an isogenic, gene-corrected iPSC line from a symptomatic 57-year-old female patient with frontotemporal dementia caused by a P301L mutation in the microtubule associated protein tau (MAPT) gene

Nimsanor, Natakarn; Kitiyanant, Narisorn; Poulsen, Ulla; Rasmussen, Mikkel A.; Clausen, Christian; Mau-Holzmann, Ulrike A.; Nielsen, Jorgen E.; Nielsen, Troels T.; Hyttel, Poul; Holst, Bjorn; Schmid, Benjamin (2016)
Generation of an isogenic, gene-corrected iPSC line from a symptomatic 59-year-old female patient with frontotemporal dementia caused by an R406W mutation in the microtubule associated protein tau (MAPT) gene

Nimsanor, Natakarn; Poulsen, Ulla; Rasmussen, Mikkel A.; Clausen, Christian; Mau-Holzmann, Ulrike A.; Nielsen, Jorgen E.; Nielsen, Troels T.; Hyttel, Poul; Holst, Bjorn; Schmid, Benjamin (2016)
Generation of induced pluripotent stem cells derived from a 77-year-old healthy woman as control for age related diseases

Nimsanor, Natakarn; Jorring, Ida; Rasmussen, Mikkel A.; Clausen, Christian; Mau-Holzmann, Ulrike A.; Bus, Christine; Hoffmann, Susanna A.; Gasser, Thomas; Kluba, Torsten; Holst, Bjorn; Schmid, Benjamin (2016)
Generation of iPSCs by Nonintegrative RNA-Based Reprogramming Techniques: Benefits of Self-Replicating RNA versus Synthetic mRNA

Steinle, Heidrun; Weber, Marbod; Behring, Andreas; Mau-Holzmann, Ulrike; Schlensak, Christian; Wendel, Hans Peter; Avci-Adali, Meltem (2019)
Generation of two gene edited iPSC-lines carrying a DOX-inducible NGN2 expression cassette with and without GFP in the AAVS1 locus

Schmid, Benjamin; Holst, Bjorn; Poulsen, Ulla; Jorring, Ida; Clausen, Christian; Rasmussen, M.; Mau-Holzmann, Ulrike A.; Steeg, Rachel; Nuthall, Hugh; Ebneth, A.; Cabrera-Socorro, A. (2021)
Genome-wide UPD screening in patients with intellectual disability

Schroeder, Christopher; Ekici, Arif Buelent; Moog, Ute; Grasshoff, Ute; Mau-Holzmann, Ulrike; Sturm, Marc; Vosseler, Vanessa; Poths, Sven; Rappold, Gudrun; Riess, Angelika; Riess, Olaf; Dufke, Andreas; Bonini, Michael (2014)

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